Senior Site Activation Specialist

Responsibilities

• Complete and negotiate standard or complex investigator site contracts and budgets for various clients.
• Assist in developing investigator grant estimates and local contracting strategies.
• Adapt contract and budget templates for clinical sites.
• Utilize and maintain contracting systems, tools, and processes according to the Scope of Work and project plan.
• Collaborate with sponsors, stakeholders, and RSU regions to deliver project scope in compliance with Site Activation plans.
• Provide specialist legal, operational, and financial contracting support for the initiation and maintenance of clinical trials.
• Assist with the creation and review of core scientific, technical, and administrative documentation.
• Ensure overall contracting efficiency and adherence to project timelines and financial goals.
• Maintain accurate internal systems, including CTMS, databases, and tracking tools.
• Mentor and coach colleagues and deliver presentations to clients as required.

Requirements

• Bachelor's Degree.
• 5 years of clinical research or other relevant experience.

About the Company

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.